SYNTHESIS OF BERYLLIAN SAPPHIRINE IN THE SYSTEM MGO-BEO-AL2O3-SIO2-H2O AND COMPARISON WITH NATURALLY OCCURRING BERYLLIAN SAPPHIRINE AND KHMARALITE, PART 2: A CHEMOGRAPHIC STUDY OF BE CONTENT AS A FUNCTION OF P, T, ASSEMBLAGE AND FEMG-1 EXCHANGE

Abstract

Beryllium is a significant constituent in sapphirine in some metamorphic and pegmatitic rocks, and thus could have a major effect on its stability relationships. Using the stoichiometries of reactions involving sapphirine and associated phases in the MgO-BeO-Al2O3-SiO2 (MBeAS) system in conjunction with molar volume data, we have plotted maps of the sapphirine solid-solution field in both μ-μ and μ-P space, where μ is the chemical potential of an exchange component such as (BeSi)(AlAl)-1. These maps give a pressure sequence of stable MBeAS univariant reactions and divariant assemblages that are consistent with experimental data, e.g., they show how Be stabilizes sapphirine + forsterite, which is rare in nature but readily synthesized over a wide P-T range in the presence of Be. We generate a MBeAS petrogenetic grid for sapphirine-bearing assemblages over the approximate range T = 700-900 °C, P = 0-2.5 GPa, identify divariant and univariant assemblages containing sapphirine with maximum Be, and determine the sense of variation of maximum Be content with P. At lower T, maximum Be occurs at the low-P limit of surinamite stability, ca. 0.5 GPa. At higher T, maximum Be increases with P, following the MBeAS univariant reactions involving (sapphirine + surinamite + orthopyroxene + chrysoberyl + forsterite or spinel). Natural assemblages containing sapphirine and its Be-rich near-analog khmaralite from the Napier Complex, Enderby Land, East Antarctica formed at higher T (900-1100 °C) than the experiments and in bulk compositions containing substantial Fe. Associated minerals include garnet, sillimanite, quartz, and magnesiotaaffeite-6N′3S ("musgravite"), whereas forsterite is absent and cordierite is a local, late phase. μ(BeSi)(AlAl)-1-μFeMg-1 diagrams show that the stability of magnesiotaaffeite-6N′3S causes the maximally beryllian khmaralite to shift from a magnesian composition in equilibrium with orthopyroxene + surinamite + forsterite + chrysoberyl, as in the MBeAS subsystem, to a more Fe-rich composition associated with garnet + surinamite + magnesiotaaffeite-6N′3S + chrysoberyl. Khmaralite associated with sillimanite + garnet + surinamite + magnesiotaaffeite-6N′3S or chrysoberyl in a Napier Complex pegmatite from Khmara Bay is predicted to be the most Be-rich possible in the presence of sillimanite, whereas the sillimanite + quartz ± orthopyroxene ± garnet associations in quartz granulites requires a sapphirine much lower in both Be and Fe: analyses are roughly in accord with these predictions. The shape of the sapphirine/khmaralite solid-solution field is such that there is a positive correlation between high Be and high Fe2+, a chemographic effect independent of any crystal chemical effects due to the clustering of Fe and Be in the crystal structure of khmaralite. The diagram for FMBeAS shows that sapphirine + quartz, which is often cited as evidence for ultrahigh temperatures (e.g., ≥ 1040 °C), is stabilized to lower T and higher P than in the corresponding Be-free system. Hence, this minimum T may be valid only in rocks with relatively abundant sapphirine and/or very low bulk Be content so that what Be is present in the system is not concentrated in sapphirine.